TN2009000142A1 - Bicyclic triazoles as protein kinase modulators - Google Patents
Bicyclic triazoles as protein kinase modulatorsInfo
- Publication number
- TN2009000142A1 TN2009000142A1 TNP2009000142A TN2009000142A TN2009000142A1 TN 2009000142 A1 TN2009000142 A1 TN 2009000142A1 TN P2009000142 A TNP2009000142 A TN P2009000142A TN 2009000142 A TN2009000142 A TN 2009000142A TN 2009000142 A1 TN2009000142 A1 TN 2009000142A1
- Authority
- TN
- Tunisia
- Prior art keywords
- protein kinase
- kinase modulators
- bicyclic triazoles
- triazoles
- bicyclic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
The present disclosure provides bicyclic triazole protein kinase modulators of formula I : and methods of using these compounds to treat diseases mediated by kinase activity.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86255206P | 2006-10-23 | 2006-10-23 | |
| US87030906P | 2006-12-15 | 2006-12-15 | |
| US91376607P | 2007-04-24 | 2007-04-24 | |
| US95284007P | 2007-07-30 | 2007-07-30 | |
| PCT/US2007/081841 WO2008051808A2 (en) | 2006-10-23 | 2007-10-18 | Bicyclic triazoles as protein kinase modulators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2009000142A1 true TN2009000142A1 (en) | 2010-10-18 |
Family
ID=38956385
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2009000142A TN2009000142A1 (en) | 2006-10-23 | 2009-04-15 | Bicyclic triazoles as protein kinase modulators |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8507489B2 (en) |
| EP (1) | EP2084162B1 (en) |
| JP (1) | JP5378222B2 (en) |
| KR (1) | KR20090071612A (en) |
| AR (1) | AR063520A1 (en) |
| AU (1) | AU2007309149C1 (en) |
| BR (1) | BRPI0717320A2 (en) |
| CA (1) | CA2667428A1 (en) |
| CO (1) | CO6190620A2 (en) |
| CR (1) | CR10803A (en) |
| DK (1) | DK2084162T3 (en) |
| EA (1) | EA200970403A1 (en) |
| ES (1) | ES2393130T3 (en) |
| IL (1) | IL197958A0 (en) |
| MA (1) | MA30871B1 (en) |
| MX (1) | MX2009004059A (en) |
| NO (1) | NO20091618L (en) |
| NZ (1) | NZ575336A (en) |
| PE (1) | PE20080893A1 (en) |
| PL (1) | PL2084162T3 (en) |
| PT (1) | PT2084162E (en) |
| SV (1) | SV2009003235A (en) |
| TN (1) | TN2009000142A1 (en) |
| TW (1) | TW200835492A (en) |
| WO (1) | WO2008051808A2 (en) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PA8792501A1 (en) * | 2007-08-09 | 2009-04-23 | Sanofi Aventis | NEW DERIVATIVES OF 6-TRIAZOLOPIRIDACINA-SULFANIL BENZOTIAZOL AND BENCIMIDAZOL, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICATIONS, PHARMACEUTICAL COMPOSITIONS AND NEW MAIN USE AS MET INHIBITORS. |
| TWI365185B (en) | 2008-07-24 | 2012-06-01 | Lilly Co Eli | Amidophenoxyindazoles useful as inhibitors of c-met |
| UY32049A (en) | 2008-08-14 | 2010-03-26 | Takeda Pharmaceutical | CMET INHIBITORS |
| EP2165710A1 (en) * | 2008-09-19 | 2010-03-24 | Institut Curie | Tyrosine kinase receptor Tyro3 as a therapeutic target in the treatment of a bladder tumor |
| JP2012509342A (en) | 2008-11-20 | 2012-04-19 | オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド | Substituted pyrrolo [2,3-B] -pyridine and -pyrazine |
| FR2941951B1 (en) * | 2009-02-06 | 2011-04-01 | Sanofi Aventis | 6- (6-NH-SUBSTITUTED-TRIAZOLOPYRIDAZINE-SULFANYL) BENZOTHIAZOLES AND BENZIMIDAZOLES DERIVATIVES: PREPARATION, APPLICATION AS MEDICAMENTS AND USE AS INHIBITORS OF MET. |
| FR2941952B1 (en) * | 2009-02-06 | 2011-04-01 | Sanofi Aventis | 6- (6-SUBSTITUTED-TRIAZOLOPYRIDAZINE-SULFANYL) DERIVATIVES 5-FLUORO-BENZOTHIAZOLES AND 5-FLUORO-BENZIMIDAZOLES: PREPARATION, APPLICATION AS MEDICAMENTS AND USE AS INHIBITORS OF MET. |
| FR2941950B1 (en) * | 2009-02-06 | 2011-04-01 | Sanofi Aventis | 6- (6-O-SUBSTITUTED-TRIAZOLOPYRIDAZINE-SULFANYL) BENZOTHIAZOLES AND BENZIMIDAZOLES DERIVATIVES: PREPARATION, APPLICATION AS MEDICAMENTS AND USE AS INHIBITORS OF MET. |
| FR2941949B1 (en) * | 2009-02-06 | 2011-04-01 | Sanofi Aventis | DERIVATIVES OF 6- (6-O-CYCLOALKYL OR 6-NH-CYCLOALKYL-TRIAZOLOPYRIDAZINE-SULFANYL) BENZOTHIAZOLES AND BENZIMIDAZOLES PREPARATION, APPLICATION AS MEDICAMENTS AND USE AS INHIBITORS OF MET. |
| WO2011018454A1 (en) | 2009-08-12 | 2011-02-17 | Novartis Ag | Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation |
| CA2771432A1 (en) | 2009-08-20 | 2011-02-24 | Novartis Ag | Heterocyclic oxime compounds |
| WO2011079804A1 (en) | 2009-12-31 | 2011-07-07 | Hutchison Medipharma Limited | Certain triazolopyridines and triazolopyrazines, compositions thereof and methods of use therefor |
| WO2011143646A1 (en) | 2010-05-14 | 2011-11-17 | OSI Pharmaceuticals, LLC | Fused bicyclic kinase inhibitors |
| AR081039A1 (en) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | QUINASA FUSIONED BICYCLE INHIBITORS |
| AR085183A1 (en) * | 2010-07-30 | 2013-09-18 | Lilly Co Eli | COMPOUND 6- (1-METHYL-1H-PIRAZOL-4-IL) -3- (2-METHYL-2H-INDAZOL-5-ILTIO) - [1,2,4] TRIAZOL [4,3-B] PIRIDAZINE, PHARMACEUTICAL COMPOSITION THAT UNDERSTAND AND USE IT TO PREPARE A USEFUL MEDICINAL PRODUCT TO TREAT CANCER |
| UY33549A (en) * | 2010-08-10 | 2012-01-31 | Glaxo Group Ltd | QUINOLIL AMINAS AS INHIBITING AGENTS OF KINASES |
| WO2012042421A1 (en) | 2010-09-29 | 2012-04-05 | Pfizer Inc. | Method of treating abnormal cell growth |
| CN102532141A (en) | 2010-12-08 | 2012-07-04 | 中国科学院上海药物研究所 | (1,2,4)-triazolo-(4,3-b) (1,2,4)-triazine compounds, as well as preparation method and use thereof |
| WO2012096929A2 (en) | 2011-01-11 | 2012-07-19 | Sunovion Pharmaceuticals Inc. | Heteroaryl compounds and methods of use thereof |
| WO2012107500A1 (en) | 2011-02-10 | 2012-08-16 | Novartis Ag | [1, 2, 4] triazolo [4, 3 -b] pyridazine compounds as inhibitors of the c-met tyrosine kinase |
| CN103459396B (en) * | 2011-02-10 | 2015-08-19 | 诺瓦提斯公司 | As [1,2,4] triazolo [4,3-b] pyridazine compound of c-Met tyrosine kinase inhibitor |
| JP2014513724A (en) | 2011-05-16 | 2014-06-05 | オーエスアイ・ファーマシューティカルズ,エルエルシー | Fusion bicyclic kinase inhibitor |
| CN103958509B (en) * | 2011-09-15 | 2015-12-23 | 诺华股份有限公司 | 6-Substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-A]pyridine compounds as tyrosine kinase inhibitors |
| WO2013038362A1 (en) | 2011-09-15 | 2013-03-21 | Novartis Ag | 6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase |
| WO2013151913A1 (en) | 2012-04-03 | 2013-10-10 | Novartis Ag | Tyrosine kinase inhibitor combinations and their use |
| RU2660354C2 (en) | 2012-04-03 | 2018-07-05 | Новартис Аг | Combined products containing tyrosine kinase inhibitors and their use |
| CN103122000B (en) * | 2012-09-03 | 2013-12-25 | 中美冠科生物技术(太仓)有限公司 | High-selectivity c-Met kinase inhibitor used as antitumor drug |
| WO2014089904A1 (en) | 2012-12-10 | 2014-06-19 | Abbvie Inc. | Triazinone compounds |
| US20150174034A1 (en) | 2013-03-13 | 2015-06-25 | Avon Products, Inc. | Tyrosinase inhibitors |
| US20150152122A1 (en) * | 2013-03-13 | 2015-06-04 | Avon Products, Inc. | Tyrosinase inhibitors |
| US9364405B2 (en) | 2013-03-13 | 2016-06-14 | Avon Products, Inc. | Tyrosinase inhibitors |
| AR095365A1 (en) * | 2013-03-13 | 2015-10-14 | Hoffmann La Roche | PROCEDURE TO PREPARE BENZOXAZEPINE COMPOUNDS |
| WO2014174478A1 (en) | 2013-04-26 | 2014-10-30 | Novartis Ag | Pharmaceutical combinations of a pkc inhibitor and a c-met receptor tyrosine kinase inhibitor |
| US9512121B2 (en) | 2013-05-10 | 2016-12-06 | Jiangsu Hansoh Pharmaceutical Co., Ltd. | [1,2,4] triazol [4,3-A] pyridine derivative, preparation method therefor or medical application thereof |
| US10301325B2 (en) | 2015-09-24 | 2019-05-28 | Shanghai Haiju Biological Technology Co., Ltd. | Quinoline derivative, and pharmaceutical composition, preparation method and use thereof |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5604091A (en) | 1984-03-01 | 1997-02-18 | Microgenics Corporation | Methods for protein binding enzyme complementation |
| JPS60194443A (en) * | 1984-03-16 | 1985-10-02 | Fuji Photo Film Co Ltd | Photosensitive silver halide material |
| EP0228061A3 (en) * | 1985-12-23 | 1988-12-14 | Takeda Chemical Industries, Ltd. | Cephem compounds |
| JPS62228086A (en) * | 1985-12-23 | 1987-10-06 | Takeda Chem Ind Ltd | Cephem compound |
| GB9918035D0 (en) | 1999-07-30 | 1999-09-29 | Novartis Ag | Organic compounds |
| WO2002083675A2 (en) * | 2001-04-10 | 2002-10-24 | Merck Sharp & Dohme Limited | Inhibitors of akt activity |
| WO2002083139A1 (en) * | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | Inhibitors of akt activity |
| US20030229453A1 (en) | 2002-04-09 | 2003-12-11 | Antonysamy Stephen Suresh | Crystals and structures of PAK4KD kinase PAK4KD |
| US7268136B2 (en) * | 2002-12-18 | 2007-09-11 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of protein kinases |
| US7122548B2 (en) * | 2003-07-02 | 2006-10-17 | Sugen, Inc. | Triazolotriazine compounds and uses thereof |
| WO2006015124A2 (en) * | 2004-07-27 | 2006-02-09 | Sgx Pharmaceuticals, Inc. | Fused ring heterocycle kinase modulators |
| SI1784396T1 (en) | 2004-08-26 | 2011-03-31 | Pfizer | Pyrazole-substituted aminoheteroaryl compounds as protein kinase inhibitors |
| KR100994173B1 (en) | 2004-12-27 | 2010-11-15 | 알콘, 인코퍼레이티드 | Aminopyrazine Analogues for Treatment of Glaucoma and Other Rho Kinase-Mediated Diseases |
-
2007
- 2007-10-18 WO PCT/US2007/081841 patent/WO2008051808A2/en not_active Ceased
- 2007-10-18 CA CA002667428A patent/CA2667428A1/en not_active Abandoned
- 2007-10-18 MX MX2009004059A patent/MX2009004059A/en active IP Right Grant
- 2007-10-18 US US12/442,566 patent/US8507489B2/en not_active Expired - Fee Related
- 2007-10-18 AU AU2007309149A patent/AU2007309149C1/en not_active Ceased
- 2007-10-18 EA EA200970403A patent/EA200970403A1/en unknown
- 2007-10-18 KR KR1020097008200A patent/KR20090071612A/en not_active Abandoned
- 2007-10-18 EP EP07844414A patent/EP2084162B1/en active Active
- 2007-10-18 ES ES07844414T patent/ES2393130T3/en active Active
- 2007-10-18 BR BRPI0717320-2A2A patent/BRPI0717320A2/en not_active IP Right Cessation
- 2007-10-18 PT PT07844414T patent/PT2084162E/en unknown
- 2007-10-18 NZ NZ575336A patent/NZ575336A/en not_active IP Right Cessation
- 2007-10-18 JP JP2009533541A patent/JP5378222B2/en not_active Expired - Fee Related
- 2007-10-18 DK DK07844414.8T patent/DK2084162T3/en active
- 2007-10-18 PL PL07844414T patent/PL2084162T3/en unknown
- 2007-10-22 TW TW096139480A patent/TW200835492A/en unknown
- 2007-10-23 AR ARP070104680A patent/AR063520A1/en not_active Application Discontinuation
- 2007-10-23 PE PE2007001437A patent/PE20080893A1/en not_active Application Discontinuation
-
2009
- 2009-04-05 IL IL197958A patent/IL197958A0/en unknown
- 2009-04-15 TN TNP2009000142A patent/TN2009000142A1/en unknown
- 2009-04-22 CO CO09040677A patent/CO6190620A2/en not_active Application Discontinuation
- 2009-04-23 SV SV2009003235A patent/SV2009003235A/en not_active Application Discontinuation
- 2009-04-23 NO NO20091618A patent/NO20091618L/en not_active Application Discontinuation
- 2009-05-07 MA MA31849A patent/MA30871B1/en unknown
- 2009-05-19 CR CR10803A patent/CR10803A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP2084162A2 (en) | 2009-08-05 |
| AU2007309149A1 (en) | 2008-05-02 |
| WO2008051808A3 (en) | 2008-07-24 |
| AU2007309149C1 (en) | 2013-04-04 |
| NZ575336A (en) | 2012-04-27 |
| PL2084162T3 (en) | 2013-01-31 |
| EP2084162B1 (en) | 2012-09-12 |
| CA2667428A1 (en) | 2008-05-02 |
| US8507489B2 (en) | 2013-08-13 |
| DK2084162T3 (en) | 2012-10-01 |
| AR063520A1 (en) | 2009-01-28 |
| SV2009003235A (en) | 2009-10-15 |
| JP2010507578A (en) | 2010-03-11 |
| BRPI0717320A2 (en) | 2013-10-22 |
| PT2084162E (en) | 2012-10-09 |
| CR10803A (en) | 2009-06-16 |
| KR20090071612A (en) | 2009-07-01 |
| WO2008051808A2 (en) | 2008-05-02 |
| NO20091618L (en) | 2009-05-22 |
| MX2009004059A (en) | 2009-04-27 |
| EA200970403A1 (en) | 2009-10-30 |
| TW200835492A (en) | 2008-09-01 |
| AU2007309149B2 (en) | 2012-09-06 |
| MA30871B1 (en) | 2009-11-02 |
| US20090258855A1 (en) | 2009-10-15 |
| IL197958A0 (en) | 2009-12-24 |
| CO6190620A2 (en) | 2010-08-19 |
| ES2393130T3 (en) | 2012-12-18 |
| PE20080893A1 (en) | 2008-08-26 |
| JP5378222B2 (en) | 2013-12-25 |
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